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Progress Toward Troger's Base Precursors.

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Author(s)
Raupach, Elizabeth A.
Advisor(s)
Lewis, David E.
Date
Feb 09, 2009
Subject(s)
Troger's base--Derivatives; Heterocyclic compounds--Synthesis; Ring formation (Chemistry); Posters
Series
USGZE AS589
Abstract
Our goal was to synthesize C2-symmetric flourescent Troger's base derivitives bearing substituents in the bridged diazocine ring from 4-amino-1,8-naphthalimide dyes. Our attempts at direct synthesis have been unsuccessful. As a result, we focused our attention on synthesizing a precursor 4-amino-1,8-naphthalimide with a functional group at the 3- position that would allow the dimerization of dye molecules, providing the structural framework of a Troger's base.
Description
Color poster with text and diagrams describing research by Elizabeth A. Raupach, advised by David E. Lewis.
Sponsor(s)
University of Wisconsin--Eau Claire Office of Research and Sponsored Programs; Petroleum Research Fund (American Chemical Society)
Permanent link
http://digital.library.wisc.edu/1793/32193 
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